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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TCF20
(C1858fs)
Duplication
(frameshift variant)
Developmental delay with variable intellectual impairment and behavioral abnormalities
GLikely pathogenic
TCF20
(P1155A)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
TCF20
(P840A)
Single nucleotide variant
(missense variant)
Developmental delay with variable intellectual impairment and behavioral abnormalities
GConflicting classifications of pathogenicity
TCF20
(Q754*)
Single nucleotide variant
(nonsense)
Developmental delay with variable intellectual impairment and behavioral abnormalities
+1 more
GPathogenic
TCF20
Deletion
(nonsense)
Developmental delay with variable intellectual impairment and behavioral abnormalities
GLikely pathogenic
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